rs9977499
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;T) | 0 | common in complete genomics |
| Make rs9977499(C;C) |
| Make rs9977499(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 27362678 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9977499 |
| dbSNP (classic) | rs9977499 |
| ClinGen | rs9977499 |
| ebi | rs9977499 |
| HLI | rs9977499 |
| Exac | rs9977499 |
| Gnomad | rs9977499 |
| Varsome | rs9977499 |
| LitVar | rs9977499 |
| Map | rs9977499 |
| PheGenI | rs9977499 |
| Biobank | rs9977499 |
| 1000 genomes | rs9977499 |
| hgdp | rs9977499 |
| ensembl | rs9977499 |
| geneview | rs9977499 |
| scholar | rs9977499 |
| rs9977499 | |
| pharmgkb | rs9977499 |
| gwascentral | rs9977499 |
| openSNP | rs9977499 |
| 23andMe | rs9977499 |
| SNPshot | rs9977499 |
| SNPdbe | rs9977499 |
| MSV3d | rs9977499 |
| GWAS Ctlg | rs9977499 |
| GMAF | 0.3788 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21546767 ]
|
| Trait | |
| Title | Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. |
| Risk Allele | |
| P-val | 0.000004 |
| Odds Ratio | 1.5700 [1.29-1.91] |
